| dc.contributor.author | Look Natasha | en_US |
| dc.contributor.author | Kramer Marianne | en_US |
| dc.contributor.author | Herbert Ben | en_US |
| dc.contributor.author | Vesey Graham | en_US |
| dc.contributor.author | Simpson-Stroot Joyce | en_US |
| dc.contributor.author | Lim Daniel | en_US |
| dc.date.accessioned | 2009-12-21T03:53:18Z | |
| dc.date.available | 2009-12-21T03:53:18Z | |
| dc.date.issued | 2007 | en_US |
| dc.identifier | 2007002461 | en_US |
| dc.identifier.citation | Kramer Marianne et al. 2007, 'Development of a Cryptosporidium oocyst assay using an automated fiber optic-based biosensor', Biomed Central, vol. 1, no. 3, pp. 1-11. | en_US |
| dc.identifier.issn | 1754-1611 | en_US |
| dc.identifier.other | C1 | en_US |
| dc.identifier.uri | http://hdl.handle.net/10453/5859 | |
| dc.description.abstract | An intestinal protozoan parasite, Cryptosporidium parvum, is a major cause of waterborne gastrointestinal disease worldwide. Detection of Cryptosporidium oocysts in potable water is a high priority for the water treatment industry to reduce potential outbreaks among the consumer populace. Anti-Cryptosporidium oocyst polyclonal and monoclonal antibodies were tested as capture and detection reagents for use in a fiber optic biosensor assay for the detection of Cryptosporidium oocysts. Antibodies were validated using enzyme-linked immunosorbent assays, flow cytometry, Western blotting and fluorescent microscopy. Oocysts could be detected at a concentration of 105 oocysts/ml when the polyclonal antibodies were used as the capture and detection reagents. When oocysts were boiled prior to detection, a ten-fold increase in sensitivity was achieved using the polyclonal antibody. Western blotting and immunofluorescence revealed that both the monoclonal and polyclonal antibodies recognize a large (>300 kDa) molecular weight mucin-like antigen present on the surface of the oocyst wall. The polyclonal antibody also reacted with a small (105 kDa) molecular weight antigen that was present in boiled samples of oocysts. Preliminary steps to design an in-line biosensor assay system have shown that oocysts would have to be concentrated from water samples and heat treated to allow detection by a biosensor assay. | en_US |
| dc.publisher | Biomed Central | en_US |
| dc.relation.isbasedon | http://dx.doi.org/10.1186/1754-1611-1-3 | en_US |
| dc.title | Development of a Cryptosporidium oocyst assay using an automated fiber optic-based biosensor | en_US |
| dc.parent | Journal of Biological Engineering | en_US |
| dc.journal.volume | 1 | en_US |
| dc.journal.number | 3 | en_US |
| dc.publocation | London, UK | en_US |
| dc.identifier.startpage | 1 | en_US |
| dc.identifier.endpage | 11 | en_US |
| dc.cauo.name | Science | en_US |